Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "E"

451 to 460 of 465 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
451	5393	EXOSC9	Exosome component 9	PCH1D, PM/Scl-75, PMSCL1, RRP45, Rrp45p, p5, p6	Cerebral atrophy, Congenital pontocerebellar hypoplasia, Osteoarthritis, Pontocerebellar hypoplasia
452	23086	EXPH5	Exophilin 5	EBS4, SLAC2-B, SLAC2B	Alzheimer disease, Clear cell renal cell carcinoma, Dementia, Epidermolysis bullosa, Estrogen-receptor negative breast cancer, Orofacial cleft, Prostate cancer, Scoliosis, Uterine fibroid
453	2131	EXT1	Exostosin glycosyltransferase 1	EXT, LGCR, LGS, TRPS2, TTV	Atrial fibrillation, Autism, Bone fracture, Breast cancer, Chondrosarcoma, Colorectal cancer, Desbuquois syndrome, Endometrial cancer, Epilepsy, Exostoses, Generalized epilepsy, Gestational diabetes, Insomnia, Leprosy, Major depressive disorder View all (7 more)
454	2132	EXT2	Exostosin glycosyltransferase 2	SOTV, SSMS	Androgenetic alopecia, 11p11.2 deletion syndrome, Desbuquois syndrome, Exostoses, Potocki-shaffer syndrome, Seizures, scoliosis, and macrocephaly/microcephaly syndrome
455	2134	EXTL1	Exostosin like glycosyltransferase 1	EXTL	Liver cirrhosis
456	2135	EXTL2	Exostosin like glycosyltransferase 2	EXTR2	Multiple sclerosis, Prostate cancer, Schizophrenia
457	2137	EXTL3	Exostosin like glycosyltransferase 3	BOTV, EXTL1L, EXTR1, ISDNA, REGR, RPR	Atrial fibrillation, Desbuquois syndrome, Skeletal dysplasia
458	2138	EYA1	EYA transcriptional coactivator and phosphatase 1	BOP, BOR, BOS1, OFC1, OTFCS	Anhydramnios, Anterior segment dysgenesis, Asymmetric crying face association, Autism, Bell's palsy, Bor syndrome, Branchiooculofacial syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Cayler cardiofacial syndrome, Obstructive pulmonary disease, Conductive hearing loss, Congenital abnormalities, Renal agenesis, Congenital heart defects View all (22 more)
459	2139	EYA2	EYA transcriptional coactivator and phosphatase 2	EAB1	Asthma, Attention deficit hyperactivity disorder, Glaucoma, Insomnia, Metabolic syndrome, Myelodysplastic syndrome, Nonalcoholic fatty liver disease, Open angle glaucoma, Osteoarthritis, Otosclerosis, Respiratory system disease, Schizophrenia, Scoliosis, Seasonal allergic rhinitis, Diabetes mellitus type 2
460	2070	EYA4	EYA transcriptional coactivator and phosphatase 4	CMD1J, DFNA10	Alzheimer disease, Asthma, Atrial fibrillation, Isolated sensorineural deafness, Nonsyndromic hearing loss, Dilated cardiomyopathy, Cardiomyopathy, Colorectal neoplasms, Congestive heart failure, Deafness, Gastroesophageal reflux disease, Hearing impairment, Hearing loss, Heart failure, Hereditary hearing loss View all (2 more)

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